50717-64-1 Usage
General Description
1-(2-aminophenyl)-3-(2-methylphenyl)thiourea is a chemical compound with the molecular formula C13H14N2S. It is a thiourea derivative with an aminophenyl group and a methylphenyl group attached to the thiourea functional group. 1-(2-aminophenyl)-3-(2-methylphenyl)thiourea has been studied for its potential pharmacological properties, including its activity as an anti-cancer and anti-inflammatory agent. It is also used in scientific research as a chemical reagent for various experimental purposes. Additionally, its structure and reactivity make it a potential candidate for further drug development and medicinal chemistry studies.
Check Digit Verification of cas no
The CAS Registry Mumber 50717-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,1 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 50717-64:
(7*5)+(6*0)+(5*7)+(4*1)+(3*7)+(2*6)+(1*4)=111
111 % 10 = 1
So 50717-64-1 is a valid CAS Registry Number.
50717-64-1Relevant articles and documents
Potassium Periodate Mediated Oxidative Cyclodesulfurization toward Benzofused Nitrogen Heterocycles
Duangkamol, Chuthamat,Pattarawarapan, Mookda,Phakhodee, Wong
, p. 1981 - 1990 (2020/07/03)
A convenient oxidative cyclodesulfurization method toward the synthesis of benzofused nitrogen heterocycles using inexpensive and readily available potassium periodate as an oxidant was developed. Upon treating isothiocyanates with ortho -substituted anilines bearing N, N -, N, O -, and N, S -bis-nucleophiles, followed by an intramolecular cyclization of the in situ generated monothioureas, substituted 2-aminobenzazole series were rapidly accessible in good to excellent yields. The protocol can accommodate various substituents on both substrates while allowing more efficient, greener, and operational simpler process relative to other oxidative coupling reactions. Tetracyclic quinazolinone derivatives were also afforded in high yields in a single preparative step and chromatography-free.
